FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 4152694 · Received October 8, 2014

Report

Report Number
9616091-2014-02122
Event Type
Malfunction
Date Received
October 8, 2014
Report Date
September 22, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES THAT THE LEFT WHEEL LOCK IS BROKEN WHERE IT ATTACHES TO THE LEFT WHEEL. NO ADDITIONAL INFORMATION PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
630386 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX SOLARA3G

Patients

Seq Age Sex Outcome Treatment
1 Other